Supratentorial primitive neuroectodermal tumor

Common Name(s)

Supratentorial primitive neuroectodermal tumor

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Supratentorial primitive neuroectodermal tumor" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Supratentorial primitive neuroectodermal tumor" returned 8 free, full-text research articles on human participants. First 3 results:

A patient tumor-derived orthotopic xenograft mouse model replicating the group 3 supratentorial primitive neuroectodermal tumor in children.
 

Author(s): Zhigang Liu, Xiumei Zhao, Yue Wang, Hua Mao, Yulun Huang, Mari Kogiso, Lin Qi, Patricia A Baxter, Tsz-Kwong Man, Adekunle Adesina, Jack M Su, Daniel Picard, King Ching Ho, Annie Huang, Laszlo Perlaky, Ching C Lau, Murali Chintagumpala, Xiao-Nan Li

Journal: Neuro-oncology. 2014 Jun;16(6):787-99.

 

Supratentorial primitive neuroectodermal tumor (sPNET) is a malignant brain tumor with poor prognosis. New model systems that replicate sPNET's molecular subtype(s) and maintain cancer stem cell (CSC) pool are needed.

Last Updated: 16 May 2014

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Supratentorial primitive neuroectodermal tumor (PNET): an uncommon location.
 

Author(s): Fabiano Reis, Guilherme Henrique Alves Vieira, Fabio Rogerio, Marilisa Mantovani Guerreiro, Luciano de Souza Queiroz, Verônica de Araújo Zanardi

Journal: Arq Neuropsiquiatr. 2011 Dec;69(6):997.

 

Last Updated: 2 Feb 2012

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Small supratentorial, extraaxial primitive neuroectodermal tumor causing large intracerebral hematoma.
 

Author(s): Jan-Karl Burkhardt, Ralf A Kockro, Hildegard Dohmen-Scheufler, Christoph M Woernle, David Bellut, Spyros Kollias, Helmut Bertalanffy

Journal: Neurol. Med. Chir. (Tokyo). 2011 ;51(6):441-4.

 

A 16-year-old boy presented with an unusual case of a supratentorial, extraaxial small round blue cell tumor of the central nervous system, which was most likely a primitive neuroectodermal tumor (PNET). Preoperative computed tomography and magnetic resonance imaging showed a large ...

Last Updated: 24 Jun 2011

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Supratentorial primitive neuroectodermal tumor" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Chemotherapy and Radiation Therapy in Treating Young Patients With Newly Diagnosed, Previously Untreated, High-Risk Medulloblastoma
 

Status: Recruiting

Condition Summary: Untreated Childhood Medulloblastoma; Untreated Childhood Pineoblastoma; Untreated Childhood Supratentorial Primitive Neuroectodermal Tumor

 

Last Updated: 19 Aug 2016

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Melphalan, Carboplatin, Mannitol, and Sodium Thiosulfate in Treating Patients With Recurrent or Progressive CNS Embryonal or Germ Cell Tumors
 

Status: Recruiting

Condition Summary: Adult Central Nervous System Germ Cell Tumor; Adult Ependymoblastoma; Adult Medulloblastoma; Adult Pineoblastoma; Adult Supratentorial Primitive Neuroectodermal Tumor; Childhood Atypical Teratoid/Rhabdoid Tumor; Childhood Central Nervous System Germ Cell Tumor; Childhood Ependymoblastoma; Medulloepithelioma; Ototoxicity; Recurrent Adult Brain Neoplasm; Recurrent Childhood Central Nervous System Embryonal Neoplasm; Recurrent Childhood Malignant Germ Cell Tumor; Recurrent Childhood Medulloblastoma; Recurrent Childhood Pineoblastoma; Recurrent Childhood Supratentorial Primitive Neuroectodermal Tumor

 

Last Updated: 7 Nov 2016

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Study of Fixed vs. Flexible Filgrastim to Accelerate Bone Marrow Recovery After Chemotherapy in Children With Cancer
 

Status: Recruiting

Condition Summary: Childhood Choroid Plexus Tumor; Childhood Medulloblastoma; Childhood Pineoblastoma; Childhood Soft Tissue Sarcoma; Childhood Supratentorial Primitive Neuroectodermal Tumor; Neuroblastoma; Osteosarcoma; Retinoblastoma; Wilms Tumor and Other Childhood Kidney Tumors; Recurrent/Refractory Childhood Hodgkin Lymphoma; Unspecified Childhood Solid Tumor, Protocol Specific

 

Last Updated: 25 Jan 2016

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